NEN-EN-ISO 11607-2
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
inactive
| Organization: | NEN |
| Publication Date: | 1 July 2017 |
| Status: | inactive |
| Page Count: | 40 |
| ICS Code (Sterilized packaging): | 11.080.30 |
scope:
NEN-EN-ISO 11607-2 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing, and assembly of preformed sterile barrier systems, sterile barrier systems and packaging systems. This part of ISO 11607 is applicable to industry, to health care facilities, and wherever medical devices are packaged and sterilized. This part of ISO 11607 does not cover all requirements for packaging medical devices that are manufactured aseptically. Additional requirements may also be necessary for drug/device combinations.
Document History
July 1, 2022
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
A description is not available for this item.
February 1, 2020
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
This document specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing and...
November 1, 2017
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
NEN-EN-ISO 11607-2 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing, and...
NEN-EN-ISO 11607-2
July 1, 2017
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
NEN-EN-ISO 11607-2 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing, and...
July 1, 2014
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
A description is not available for this item.
April 1, 2013
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
A description is not available for this item.
May 1, 2006
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing,...
May 1, 2004
Packaging for terminally sterilized medical devices - Part 2: Requirements for forming and sealing and assembly processes
This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing,...